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nsv4266471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:890

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 22 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):50,588,637-50,589,526Question Mark
Overlapping variant regions from other studies: 21 SVs from 6 studies. See in: genome view    
Submitted genomic48,665,998-48,666,887Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4266471RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1750,588,63750,589,526
nsv4266471Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1748,665,99848,666,887

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15835139deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15835139RemappedPerfectNC_000017.11:g.505
88637_50589526del
GRCh38.p12First PassNC_000017.11Chr1750,588,63750,589,526
nssv15835139Submitted genomicNC_000017.10:g.486
65998_48666887del
GRCh37.p13NC_000017.10Chr1748,665,99848,666,887

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv15835139<0.0011521694
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